ClinGen Allele Registry
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Canonical Allele Identifier:
CA87625120
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765306C>T
GRCh37
chr3:g.169483094C>T
Linked Data - NCBI & NCI
dbSNP:
982381707
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765306C>T , CM000665.2:g.169765306C>T
GRCh38
NC_000003.11:g.169483094C>T , CM000665.1:g.169483094C>T
GRCh37
NC_000003.10:g.170965788C>T
NCBI36
NG_016363.1:g.4755G>A , LRG_347:g.4755G>A
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